(Q72730388)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

title

A new type of peroxisomal disorder with variable expression in liver and fibroblasts (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

author name string

H Mandel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

M Espeel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

F Roels

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

N Sofer

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

A Luder

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

T C Iancu

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

A Aizin

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

M Berant

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

R J Wanders

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

R B Schutgens

10

1 reference

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28 October 2019

language of work or name

English

0 references

publication date

1 October 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

28 October 2019

published in

1 reference

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28 October 2019

volume

125

1 reference

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28 October 2019

issue

4

1 reference

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28 October 2019

page(s)

549-555

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

Peroxisomal disorders in neurology

28 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Bile acids in peroxisomal disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Peroxisomal functions in classical Refsum's disease: comparison with the infantile form of Refsum's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Light microscopic visualization of peroxisomes and plasmalogens in first trimester chorionic villi

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Human liver pathology in peroxisomal diseases: a review including novel data

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Ataxia and peripheral neuropathy: a benign variant of peroxisome dysgenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Peroxisomal disorders: clinical characterization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

In vivo and vitro studies on formation of bile acids in patients with Zellweger syndrome. Evidence that peroxisomes are of importance in the normal biosynthesis of both cholic and chenodeoxycholic acid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Pseudo infantile Refsum's disease: catalase-deficient peroxisomal particles with partial deficiency of plasmalogen synthesis and oxidation of fatty acids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Catalase-negative peroxisomes in human embryonic liver

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

The development of microperoxisomes in the cells of the proximal tubules of the kidney and epithelium of the small intestine during the embryonic development and postnatal period

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Peroxisome through cell differentiation and neoplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

The extracellular matrix coordinately modulates liver transcription factors and hepatocyte morphology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Stem cell biology, hormone/matrix synergies and liver differentiation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

Prenatal diagnosis of Zellweger syndrome by determination of trihydroxycoprostanic acid in amniotic fluid

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2894%2970006-0

10.1016/S0022-3476(94)70006-0

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7931872%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1 reference